Supplementary Material for: CAPOS and Beyond: ATP1A3 Variants in Pediatric Movement Disorders: Case Reports

Supplementary Material for: CAPOS and Beyond: ATP1A3 Variants in Pediatric Movement Disorders: Case Reports

Introduction: ATP1A3-related disorders encompass a clinically heterogeneous spectrum that includes previously defined dominantly inherited phenotypes such as Alternating Hemiplegia of Childhood (AHC), Rapid-Onset Dystonia-Parkinsonism (RDP), and cerebellar ataxia, areflexia, pes cavus, optic atrophy...

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主要作者:	figshare admin karger (2628495) (author)
其他作者:	SarıYanartaş M. (22687652) (author), YayıcıKöken Ö. (22687655) (author), Ceylan A.C. (22687658) (author), Bozacı A.E. (22687661) (author), TuralKara T. (22687664) (author), Haspolat Ş. (22687667) (author)
出版:	2025
主题:	Medicine
标签:	添加标签没有标签, 成为第一个标记此记录!

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